Cleared Traditional

K954827 - SEALITE FL

K954827 is the FDA 510(k) clearance for SEALITE FL by Sybron Dental Specialties, Inc.. It is a Class 2 Dental device (product code EBC) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K954827 · Sybron Dental Specialties, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1996
Decision
76d
Days
Class 2
Risk

K954827 is an FDA 510(k) clearance for the SEALITE FL. Classified as Sealant, Pit And Fissure, And Conditioner (product code EBC), Class II - Special Controls.

Submitted by Sybron Dental Specialties, Inc. (Glendora, US). The FDA issued a Cleared decision on January 4, 1996 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3765 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Sybron Dental Specialties, Inc. devices

Submission Details

510(k) Number K954827 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 20, 1995
Decision Date January 04, 1996
Days to Decision 76 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 127d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EBC Sealant, Pit And Fissure, And Conditioner
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3765
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - EBC Sealant, Pit And Fissure, And Conditioner

All 58
Devices cleared under the same product code (EBC) and FDA review panel - the closest regulatory comparables to K954827.
DELTON FS DIRECT DELIVERY SYSTEM
K982564 · Dentsply Intl. · Oct 1998
PULPDENT SEAL-RITE UDMA
K963921 · Pulpdent Corp. · Nov 1996
GLY-ETCH
K961190 · Centrix, Inc. · Apr 1996
TOOTH PREPARATION CONDITIONER, PRE-IMPRESSION
K952240 · Jeneric/Pentron, Inc. · Aug 1995
DELTON F PIT & FISSURE SEALANT
K951296 · Dentsply Intl. · May 1995
PULPDENT CHEMICAL CURE PIT AND FISSURE SEALANT
K945378 · Pulpdent Corp. · Jan 1995